3. 结构
3.1 二维结构
3.2 三维结构
-1
-2
-3
25 25 0 1 0 0 0 0 0999 V2000
-3.6121 -0.7382 0.6634 O 0 0 0 0 0 0 0 0 0 0 0 0
-2.0903 0.5581 1.7447 O 0 0 0 0 0 0 0 0 0 0 0 0
3.0688 1.3218 0.9145 O 0 5 0 0 0 0 0 0 0 0 0 0
1.2262 2.2458 0.1593 O 0 0 0 0 0 0 0 0 0 0 0 0
-0.4274 1.5110 -2.1025 N 0 0 0 0 0 0 0 0 0 0 0 0
1.9246 1.2351 0.4094 N 0 3 0 0 0 0 0 0 0 0 0 0
-0.7209 0.9868 -0.7636 C 0 0 2 0 0 0 0 0 0 0 0 0
0.1479 -0.2185 -0.4498 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.2224 0.6745 -0.6675 C 0 0 0 0 0 0 0 0 0 0 0 0
1.4016 -0.0530 0.1096 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.3580 -1.4727 -0.7422 C 0 0 0 0 0 0 0 0 0 0 0 0
2.1763 -1.1794 0.3862 C 0 0 0 0 0 0 0 0 0 0 0 0
0.4169 -2.5990 -0.4654 C 0 0 0 0 0 0 0 0 0 0 0 0
-2.6152 0.1803 0.7053 C 0 0 0 0 0 0 0 0 0 0 0 0
1.6840 -2.4525 0.0987 C 0 0 0 0 0 0 0 0 0 0 0 0
-0.6695 1.7739 -0.0142 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.8056 1.5900 -0.8398 H 0 0 0 0 0 0 0 0 0 0 0 0
-2.5583 -0.0336 -1.4333 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.3185 -1.6456 -1.2112 H 0 0 0 0 0 0 0 0 0 0 0 0
-1.0190 2.3205 -2.2882 H 0 0 0 0 0 0 0 0 0 0 0 0
-0.6803 0.8176 -2.8063 H 0 0 0 0 0 0 0 0 0 0 0 0
3.1683 -1.1075 0.8248 H 0 0 0 0 0 0 0 0 0 0 0 0
0.0374 -3.5902 -0.6962 H 0 0 0 0 0 0 0 0 0 0 0 0
2.2877 -3.3298 0.3121 H 0 0 0 0 0 0 0 0 0 0 0 0
-3.8553 -1.0556 1.5592 H 0 0 0 0 0 0 0 0 0 0 0 0
1 14 1 0 0 0 0
1 25 1 0 0 0 0
2 14 2 0 0 0 0
3 6 1 0 0 0 0
4 6 2 0 0 0 0
5 7 1 0 0 0 0
5 20 1 0 0 0 0
5 21 1 0 0 0 0
6 10 1 0 0 0 0
7 8 1 0 0 0 0
7 9 1 0 0 0 0
7 16 1 0 0 0 0
8 10 1 0 0 0 0
8 11 2 0 0 0 0
9 14 1 0 0 0 0
9 17 1 0 0 0 0
9 18 1 0 0 0 0
10 12 2 0 0 0 0
11 13 1 0 0 0 0
11 19 1 0 0 0 0
12 15 1 0 0 0 0
12 22 1 0 0 0 0
13 15 2 0 0 0 0
13 23 1 0 0 0 0
15 24 1 0 0 0 0
M CHG 2 3 -1 6 1
4. 国际命名与标识
4.1 IUPAC Name
(3S)-3-amino-3-(2-nitrophenyl)propanoic acid
4.2 InChl
InChI=1S/C9H10N2O4/c10-7(5-9(12)13)6-3-1-2-4-8(6)11(14)15/h1-4,7H,5,10H2,(H,12,13)/t7-/m0/s1
4.3 InChlKey
XXBOYULKNZTOMN-ZETCQYMHSA-N
4.4 Canonical SMILES
C1=CC=C(C(=C1)C(CC(=O)O)N)[N+](=O)[O-]
4.5 lsomeric SMILES
C1=CC=C(C(=C1)[C@H](CC(=O)O)N)[N+](=O)[O-]
4.6 SDF文件
5. 波谱数据
5.1 13C核磁共振谱(13C NMR)
5.2 1H核磁共振谱(1H NMR)
5.3 质谱(MS)
5.4 红外光谱(IR)
5.5 紫外/可见光谱(UV/Vis)
6. 相关药材
7. 相关靶点
8. 相关疾病